Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83786 |
| ensemblid | ENSG00000126391.14 |
| hgncid | 25462 |
| symbol | FRMD8 |
| name | FERM domain containing 8 |
| refseq_nuc | NM_031904.5 |
| refseq_prot | NP_114110.1 |
| ensembl_nuc | ENST00000317568.10 |
| ensembl_prot | ENSP00000319726.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 65386637 |
| end | 65413525 |
| strand | + |
| ver | v1.2 |
| region | chr11:65386637-65413525 |
| region5000 | chr11:65381637-65418525 |
| regionname0 | FRMD8_chr11_65386637_65413525 |
| regionname5000 | FRMD8_chr11_65381637_65418525 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 464 | 340 | 87 | 58 | 141 | 12 | 40 | 104 | FRMD8_chr11_65381637_65418525 | FRMD8 | MDGTE others(459): Show |
chr11 | 65381637 | 65418525 |
| a0002 | 0/0 | 464 | 13 | 0 | 0 | 13 | 0 | 0 | 12 | FRMD8_chr11_65381637_65418525 | FRMD8 | MDGTE others(459): Show |
chr11 | 65381637 | 65418525 |
| a0003 | 0/0 | 464 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | FRMD8_chr11_65381637_65418525 | FRMD8 | MDGTE others(459): Show |
chr11 | 65381637 | 65418525 |
| a0004 | 0/0 | 464 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | MDGTE others(459): Show |
chr11 | 65381637 | 65418525 |
| a0005 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | MDGTE others(459): Show |
chr11 | 65381637 | 65418525 |
| a0006 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | MDGTE others(459): Show |
chr11 | 65381637 | 65418525 |
| a0007 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | MDGTE others(459): Show |
chr11 | 65381637 | 65418525 |
| a0008 | 0/0 | 464 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | MDGTE others(459): Show |
chr11 | 65381637 | 65418525 |
| a0009 | 0/0 | 464 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | MDGTE others(459): Show |
chr11 | 65381637 | 65418525 |
| a0010 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | MDGTE others(459): Show |
chr11 | 65381637 | 65418525 |
| a0011 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | MDGTE others(459): Show |
chr11 | 65381637 | 65418525 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1392 | 111 | 41 | 9 | 45 | 3 | 11 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0001c0002 | 0/0 | 1392 | 94 | 21 | 10 | 51 | 2 | 10 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0001c0003 | 0/0 | 1392 | 74 | 2 | 22 | 32 | 6 | 12 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0001c0004 | 0/0 | 1392 | 29 | 9 | 4 | 9 | 1 | 6 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0001c0005 | 0/0 | 1392 | 13 | 0 | 11 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0001c0007 | 0/0 | 1392 | 12 | 12 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0001c0010 | 0/0 | 1392 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0001c0011 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0001c0012 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0001c0014 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0001c0019 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0001c0020 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0002c0006 | 0/0 | 1392 | 13 | 0 | 0 | 13 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0003c0008 | 0/0 | 1392 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0004c0009 | 0/0 | 1392 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0005c0013 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0006c0015 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0007c0017 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0008c0022 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0009c0021 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0010c0016 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 | ||
| a0011c0018 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | ATGGA others(1387): Show |
chr11 | 65381637 | 65418525 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3686 | 92 | 28 | 6 | 43 | 3 | 11 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0001t0002 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0001t0004 | 1/0 | 3685 | 11 | 8 | 2 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3680): Show |
chr11 | 65381637 | 65418525 |
| a0001c0001t0009 | 0/0 | 3686 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0001t0010 | 0/0 | 3685 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3680): Show |
chr11 | 65381637 | 65418525 |
| a0001c0001t0016 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0001t0018 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0001t0019 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0002t0001 | 0/0 | 3686 | 79 | 13 | 5 | 50 | 1 | 10 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0002t0005 | 0/0 | 3686 | 7 | 1 | 5 | 0 | 1 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0002t0008 | 0/0 | 3686 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0002t0011 | 0/0 | 3686 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0002t0020 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0002t0021 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0003t0001 | 0/0 | 3686 | 61 | 2 | 14 | 29 | 4 | 12 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0003t0006 | 0/0 | 3686 | 6 | 0 | 5 | 0 | 1 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0003t0007 | 0/0 | 3686 | 4 | 0 | 2 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0003t0014 | 0/0 | 3686 | 2 | 0 | 1 | 0 | 1 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0003t0017 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0004t0001 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0004t0002 | 0/0 | 3686 | 21 | 6 | 4 | 6 | 1 | 4 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0004t0009 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0004t0012 | 0/0 | 3686 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0004t0015 | 0/0 | 3686 | 2 | 0 | 0 | 0 | 0 | 2 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0004t0022 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0005t0002 | 0/0 | 3686 | 13 | 0 | 11 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0007t0003 | 0/0 | 3686 | 11 | 11 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0007t0013 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0010t0001 | 0/0 | 3686 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0011t0003 | 0/0 | 3686 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0012t0001 | 0/0 | 3686 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0014t0009 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0019t0002 | 0/0 | 3686 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0001c0020t0013 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0002c0006t0001 | 0/0 | 3686 | 13 | 0 | 0 | 13 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0003c0008t0001 | 0/0 | 3686 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0004c0009t0001 | 0/0 | 3686 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0005c0013t0001 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0006c0015t0001 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0007c0017t0001 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0008c0022t0001 | 0/0 | 3686 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0009c0021t0001 | 0/0 | 3686 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0010c0016t0001 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| a0011c0018t0001 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | GTCGC others(3681): Show |
chr11 | 65381637 | 65418525 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 29 | 11 | 3 | 10 | 1 | 4 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0007 | 0/0 | 6 | 1 | 0 | 3 | 2 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0121 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0004g0009 | 1/0 | 5 | 3 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0009g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0016g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0018g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0001t0019g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0003 | 0/0 | 7 | 0 | 2 | 2 | 0 | 3 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0005g0010 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0008g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0011g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0011g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0011g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0020g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0002t0021g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0002 | 0/0 | 23 | 0 | 8 | 8 | 1 | 6 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0024 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0006g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0006g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0007g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0007g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0014g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0014g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0003t0017g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0006 | 0/0 | 6 | 2 | 2 | 0 | 1 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0012g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0012g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0015g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0015g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0004t0022g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0005t0002g0004 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0005t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0005t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0005t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0005t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0005t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0007t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0007t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0007t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0007t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0007t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0007t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0007t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0007t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0007t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0010t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0011t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0012t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0014t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0019t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0001c0020t0013g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0002c0006t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0002c0006t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0002c0006t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0002c0006t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0002c0006t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0003c0008t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0003c0008t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0003c0008t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0004c0009t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0004c0009t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0005c0013t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0006c0015t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0007c0017t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0008c0022t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0009c0021t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0010c0016t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| a0011c0018t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0002 | g0006 | EUR | GBR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00140 | hp1 | a0001 | c0003 | t0006 | g0022 | EUR | GBR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0046 | EUR | GBR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0002 | EUR | FIN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0185 | EUR | FIN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00323 | hp2 | a0001 | c0003 | t0014 | g0193 | EUR | FIN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00408 | hp1 | a0001 | c0004 | t0012 | g0036 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00408 | hp2 | a0003 | c0008 | t0001 | g0001 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00438 | hp2 | a0001 | c0004 | t0002 | g0100 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0194 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00735 | hp1 | a0001 | c0002 | t0005 | g0010 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00735 | hp2 | a0001 | c0005 | t0002 | g0197 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG00741 | hp2 | a0001 | c0004 | t0002 | g0006 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01069 | hp1 | a0001 | c0002 | t0005 | g0010 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01069 | hp2 | a0001 | c0003 | t0007 | g0047 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01070 | hp2 | a0001 | c0005 | t0002 | g0004 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01071 | hp2 | a0001 | c0003 | t0007 | g0047 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01074 | hp1 | a0001 | c0003 | t0006 | g0022 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01074 | hp2 | a0001 | c0005 | t0002 | g0196 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01081 | hp1 | a0001 | c0005 | t0002 | g0004 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01081 | hp2 | a0001 | c0003 | t0006 | g0022 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0104 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0054 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01167 | hp1 | a0001 | c0004 | t0002 | g0092 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0179 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01168 | hp1 | a0001 | c0003 | t0006 | g0176 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01168 | hp2 | a0001 | c0002 | t0005 | g0010 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01169 | hp2 | a0001 | c0002 | t0005 | g0138 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01192 | hp1 | a0001 | c0005 | t0002 | g0004 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01192 | hp2 | a0001 | c0002 | t0005 | g0010 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01243 | hp2 | a0001 | c0011 | t0003 | g0205 | AMR | PUR | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01255 | hp2 | a0001 | c0003 | t0014 | g0002 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0192 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01258 | hp2 | a0001 | c0003 | t0006 | g0023 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01358 | hp1 | a0001 | c0004 | t0002 | g0091 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01361 | hp1 | a0001 | c0004 | t0002 | g0006 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0184 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0046 | EUR | IBS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01891 | hp1 | a0001 | c0004 | t0002 | g0067 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0183 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01934 | hp1 | a0001 | c0005 | t0002 | g0004 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01943 | hp1 | a0001 | c0005 | t0002 | g0195 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02004 | hp1 | a0001 | c0012 | t0001 | g0171 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02004 | hp2 | a0001 | c0005 | t0002 | g0004 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02027 | hp1 | a0001 | c0010 | t0001 | g0028 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02071 | hp2 | a0001 | c0004 | t0012 | g0036 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02083 | hp1 | a0001 | c0004 | t0002 | g0096 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02129 | hp2 | a0003 | c0008 | t0001 | g0120 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02145 | hp2 | a0001 | c0004 | t0002 | g0066 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02155 | hp2 | a0001 | c0010 | t0001 | g0028 | EAS | CDX | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | CDX | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02257 | hp2 | a0001 | c0007 | t0003 | g0207 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02258 | hp1 | a0001 | c0007 | t0003 | g0015 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02273 | hp2 | a0001 | c0005 | t0002 | g0004 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02280 | hp1 | a0001 | c0004 | t0022 | g0200 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02280 | hp2 | a0001 | c0007 | t0003 | g0015 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02293 | hp1 | a0001 | c0003 | t0006 | g0023 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02293 | hp2 | a0001 | c0005 | t0002 | g0004 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02300 | hp2 | a0001 | c0005 | t0002 | g0004 | AMR | PEL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02572 | hp1 | a0001 | c0007 | t0003 | g0015 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02572 | hp2 | a0001 | c0002 | t0008 | g0018 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02602 | hp2 | a0001 | c0004 | t0002 | g0095 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02615 | hp2 | a0001 | c0002 | t0008 | g0018 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0162 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02622 | hp2 | a0006 | c0015 | t0001 | g0001 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02647 | hp1 | a0001 | c0001 | t0018 | g0115 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02683 | hp2 | a0001 | c0004 | t0002 | g0035 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02698 | hp1 | a0001 | c0019 | t0002 | g0006 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0065 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02895 | hp1 | a0001 | c0004 | t0002 | g0006 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02896 | hp2 | a0001 | c0002 | t0008 | g0018 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02965 | hp1 | a0001 | c0007 | t0003 | g0209 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02965 | hp2 | a0007 | c0017 | t0001 | g0134 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02976 | hp1 | a0001 | c0004 | t0009 | g0055 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0137 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03041 | hp1 | a0004 | c0009 | t0001 | g0146 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03098 | hp2 | a0001 | c0007 | t0003 | g0201 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03139 | hp1 | a0004 | c0009 | t0001 | g0145 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03139 | hp2 | a0001 | c0007 | t0003 | g0015 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03209 | hp2 | a0001 | c0004 | t0002 | g0006 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03225 | hp1 | a0001 | c0007 | t0003 | g0208 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03225 | hp2 | a0001 | c0007 | t0003 | g0203 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03239 | hp2 | a0001 | c0004 | t0002 | g0006 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03453 | hp1 | a0001 | c0001 | t0019 | g0133 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03453 | hp2 | a0001 | c0002 | t0011 | g0167 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0187 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03516 | hp1 | a0001 | c0007 | t0003 | g0202 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03516 | hp2 | a0001 | c0004 | t0002 | g0077 | AFR | ESN | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03654 | hp2 | a0008 | c0022 | t0001 | g0003 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0140 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0177 | SAS | PJL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0165 | SAS | BEB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | BEB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0186 | SAS | BEB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | BEB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | STU | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | BEB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG04199 | hp1 | a0001 | c0004 | t0015 | g0097 | SAS | STU | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0148 | SAS | STU | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0189 | SAS | STU | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG04228 | hp1 | a0009 | c0021 | t0001 | g0014 | SAS | STU | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG04228 | hp2 | a0001 | c0004 | t0002 | g0035 | SAS | STU | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18522 | hp1 | a0001 | c0002 | t0011 | g0168 | AFR | YRI | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18612 | hp1 | a0002 | c0006 | t0001 | g0008 | EAS | CHB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18612 | hp2 | a0001 | c0002 | t0021 | g0068 | EAS | CHB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | CHB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18906 | hp1 | a0001 | c0004 | t0002 | g0064 | AFR | YRI | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18941 | hp2 | a0010 | c0016 | t0001 | g0057 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18942 | hp1 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18946 | hp1 | a0001 | c0004 | t0002 | g0105 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18947 | hp2 | a0002 | c0006 | t0001 | g0012 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18954 | hp2 | a0001 | c0004 | t0002 | g0099 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18956 | hp2 | a0002 | c0006 | t0001 | g0008 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18959 | hp2 | a0002 | c0006 | t0001 | g0109 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18965 | hp2 | a0002 | c0006 | t0001 | g0160 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18971 | hp1 | a0002 | c0006 | t0001 | g0012 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18971 | hp2 | a0001 | c0004 | t0002 | g0090 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18980 | hp1 | a0001 | c0005 | t0002 | g0199 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18981 | hp1 | a0001 | c0005 | t0002 | g0198 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0170 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18989 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18997 | hp1 | a0002 | c0006 | t0001 | g0008 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18997 | hp2 | a0001 | c0003 | t0001 | g0172 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA18999 | hp2 | a0003 | c0008 | t0001 | g0001 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19000 | hp1 | a0002 | c0006 | t0001 | g0012 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19002 | hp1 | a0001 | c0004 | t0002 | g0098 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19009 | hp1 | a0001 | c0003 | t0007 | g0002 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19010 | hp1 | a0002 | c0006 | t0001 | g0012 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19010 | hp2 | a0001 | c0004 | t0012 | g0093 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19011 | hp1 | a0011 | c0018 | t0001 | g0084 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19030 | hp1 | a0001 | c0002 | t0011 | g0169 | AFR | LWK | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | LWK | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0164 | AFR | LWK | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19054 | hp1 | a0002 | c0006 | t0001 | g0127 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19057 | hp1 | a0002 | c0006 | t0001 | g0008 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19057 | hp2 | a0001 | c0003 | t0001 | g0173 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19062 | hp1 | a0001 | c0003 | t0001 | g0188 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19065 | hp2 | a0001 | c0003 | t0007 | g0002 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0190 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19072 | hp1 | a0003 | c0008 | t0001 | g0037 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19076 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19080 | hp2 | a0002 | c0006 | t0001 | g0008 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19081 | hp1 | a0002 | c0006 | t0001 | g0008 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0191 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19086 | hp1 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19088 | hp1 | a0001 | c0001 | t0016 | g0040 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19089 | hp2 | a0001 | c0003 | t0017 | g0002 | EAS | JPT | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | YRI | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ASW | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA20129 | hp2 | a0001 | c0020 | t0013 | g0078 | AFR | ASW | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA20805 | hp1 | a0001 | c0002 | t0005 | g0141 | EUR | TSI | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0157 | EUR | TSI | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA20905 | hp1 | a0001 | c0004 | t0015 | g0094 | SAS | GIH | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0023 | SAS | GIH | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02109 | hp1 | a0005 | c0013 | t0001 | g0080 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02559 | hp1 | a0001 | c0007 | t0013 | g0204 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG02559 | hp2 | a0001 | c0002 | t0005 | g0010 | AFR | ACB | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG06807 | hp1 | a0001 | c0001 | t0010 | g0163 | AFR | USA | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| HG06807 | hp2 | a0001 | c0014 | t0009 | g0161 | AFR | USA | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA20300 | hp1 | a0001 | c0007 | t0003 | g0206 | AFR | USA | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| NA20300 | hp2 | a0001 | c0002 | t0020 | g0079 | AFR | USA | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0121 | REF | REF | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0009 | REF | REF | FRMD8_chr11_65381637_65418525 | FRMD8 | chr11 | 65381637 | 65418525 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:65387089 | A | C | 1 | a0002 | 13 | NA18612.hp1 NA18947.hp2 NA18956.hp2 others(10): Show |
missense_variant | MODERATE | c.53A>C | p.His18Pro | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/11 | 178/3685 | 53/1395 | 18/464 | chr11 | 65387089 | |||
| chr11:65389364 | C | G | 1 | a0003 | 4 | HG00408.hp2 HG02129.hp2 NA18999.hp2 others(1): Show |
missense_variant | MODERATE | c.89C>G | p.Ala30Gly | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/11 | 214/3685 | 89/1395 | 30/464 | chr11 | 65389364 | |||
| chr11:65393624 | C | T | 1 | a0008 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.305C>T | p.Pro102Leu | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 4/11 | 430/3685 | 305/1395 | 102/464 | chr11 | 65393624 | |||
| chr11:65396935 | G | T | 1 | a0009 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.718G>T | p.Val240Phe | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/11 | 843/3685 | 718/1395 | 240/464 | chr11 | 65396935 | |||
| chr11:65399761 | G | C | 1 | a0005 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.829G>C | p.Asp277His | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 8/11 | 954/3685 | 829/1395 | 277/464 | chr11 | 65399761 | |||
| chr11:65400811 | G | T | 1 | a0007 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1015G>T | p.Asp339Tyr | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/11 | 1140/3685 | 1015/1395 | 339/464 | chr11 | 65400811 | |||
| chr11:65404916 | C | T | 1 | a0011 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.1124C>T | p.Ala375Val | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/11 | 1249/3685 | 1124/1395 | 375/464 | chr11 | 65404916 | |||
| chr11:65404958 | C | T | 1 | a0004 | 2 | HG03041.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.1166C>T | p.Ser389Leu | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/11 | 1291/3685 | 1166/1395 | 389/464 | chr11 | 65404958 | |||
| chr11:65404990 | C | T | 1 | a0010 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.1198C>T | p.Arg400Cys | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/11 | 1323/3685 | 1198/1395 | 400/464 | chr11 | 65404990 | |||
| chr11:65405002 | C | T | 1 | a0006 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1210C>T | p.Arg404Trp | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/11 | 1335/3685 | 1210/1395 | 404/464 | chr11 | 65405002 | |||
| chr11:65411293 | G | A | 1 | a0010 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.1328G>A | p.Arg443Gln | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 1453/3685 | 1328/1395 | 443/464 | chr11 | 65411293 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:65389395 | G | A | 2 | a0001c0007 a0001c0011 |
13 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
synonymous_variant | LOW | c.120G>A | p.Thr40Thr | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/11 | 245/3685 | 120/1395 | 40/464 | chr11 | 65389395 | |||
| chr11:65389527 | G | A | 1 | a0001c0012 | 1 | HG02004.hp1 | splice_region_variant&synonymous_variant | LOW | c.252G>A | p.Leu84Leu | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/11 | 377/3685 | 252/1395 | 84/464 | chr11 | 65389527 | |||
| chr11:65393658 | C | T | 4 | a0001c0003 a0001c0010 a0001c0012 others(1): Show |
78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
synonymous_variant | LOW | c.339C>T | p.Asp113Asp | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 4/11 | 464/3685 | 339/1395 | 113/464 | chr11 | 65393658 | |||
| chr11:65394054 | G | A | 1 | a0001c0005 | 13 | HG00735.hp2 HG01070.hp2 HG01074.hp2 others(10): Show |
synonymous_variant | LOW | c.369G>A | p.Leu123Leu | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 5/11 | 494/3685 | 369/1395 | 123/464 | chr11 | 65394054 | |||
| chr11:65394348 | C | T | 1 | a0001c0020 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.504C>T | p.Cys168Cys | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/11 | 629/3685 | 504/1395 | 168/464 | chr11 | 65394348 | |||
| chr11:65394360 | C | T | 1 | a0001c0011 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.516C>T | p.Gly172Gly | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/11 | 641/3685 | 516/1395 | 172/464 | chr11 | 65394360 | |||
| chr11:65396886 | C | T | 3 | a0001c0004 a0001c0005 a0001c0019 |
43 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(40): Show |
synonymous_variant | LOW | c.669C>T | p.Ala223Ala | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/11 | 794/3685 | 669/1395 | 223/464 | chr11 | 65396886 | |||
| chr11:65400759 | G | A | 1 | a0001c0014 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.963G>A | p.Ser321Ser | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/11 | 1088/3685 | 963/1395 | 321/464 | chr11 | 65400759 | |||
| chr11:65400810 | C | T | 6 | a0001c0002 a0001c0010 a0004c0009 others(3): Show |
101 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(98): Show |
synonymous_variant | LOW | c.1014C>T | p.Phe338Phe | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/11 | 1139/3685 | 1014/1395 | 338/464 | chr11 | 65400810 | |||
| chr11:65411339 | C | T | 1 | a0001c0019 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.1374C>T | p.Gly458Gly | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 1499/3685 | 1374/1395 | 458/464 | chr11 | 65411339 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:65386670 | G | T | 1 | a0001c0004t0022 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-92G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 1/11 | 367 | chr11 | 65386670 | ||||||
| chr11:65386674 | G | C | 1 | a0001c0001t0016 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-88G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 1/11 | 363 | chr11 | 65386674 | ||||||
| chr11:65411396 | G | T | 1 | a0001c0002t0021 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*36G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 36 | chr11 | 65411396 | ||||||
| chr11:65411433 | C | T | 1 | a0001c0002t0020 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*73C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 73 | chr11 | 65411433 | ||||||
| chr11:65411461 | G | A | 1 | a0001c0002t0008 | 3 | HG02572.hp2 HG02615.hp2 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*101G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 101 | chr11 | 65411461 | ||||||
| chr11:65411496 | C | T | 1 | a0001c0002t0020 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*136C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 136 | chr11 | 65411496 | ||||||
| chr11:65411568 | C | T | 1 | a0001c0004t0012 | 3 | HG00408.hp1 HG02071.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*208C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 208 | chr11 | 65411568 | ||||||
| chr11:65411584 | C | G | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0016 others(33): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
3_prime_UTR_variant | MODIFIER | c.*224C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 224 | chr11 | 65411584 | ||||||
| chr11:65411945 | A | G | 1 | a0001c0002t0011 | 3 | HG03453.hp2 NA18522.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*585A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 585 | chr11 | 65411945 | ||||||
| chr11:65411965 | C | T | 6 | a0001c0001t0002 a0001c0004t0002 a0001c0004t0012 others(3): Show |
41 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*605C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 605 | chr11 | 65411965 | ||||||
| chr11:65412226 | C | T | 1 | a0001c0002t0011 | 3 | HG03453.hp2 NA18522.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*866C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 866 | chr11 | 65412226 | ||||||
| chr11:65412245 | G | A | 1 | a0001c0001t0001 | 2 | HG00438.hp1 HG02015.hp2 |
3_prime_UTR_variant | MODIFIER | c.*885G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 885 | chr11 | 65412245 | ||||||
| chr11:65412342 | T | TA | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(39): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
3_prime_UTR_variant | MODIFIER | c.*983dupA | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 984 | INFO_REALIGN_3_PRIME | chr11 | 65412342 | |||||
| chr11:65412358 | T | C | 1 | a0001c0003t0017 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 998 | chr11 | 65412358 | ||||||
| chr11:65412506 | C | T | 2 | a0001c0007t0003 a0001c0011t0003 |
12 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1146C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 1146 | chr11 | 65412506 | ||||||
| chr11:65412656 | C | T | 1 | a0001c0002t0005 | 7 | HG00735.hp1 HG01069.hp1 HG01168.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1296C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 1296 | chr11 | 65412656 | ||||||
| chr11:65412910 | G | A | 1 | a0001c0001t0018 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1550G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 1550 | chr11 | 65412910 | ||||||
| chr11:65412914 | T | C | 1 | a0001c0004t0015 | 2 | HG04199.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1554T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 1554 | chr11 | 65412914 | ||||||
| chr11:65413065 | C | T | 1 | a0001c0001t0010 | 3 | HG02622.hp1 HG06807.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1705C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 1705 | chr11 | 65413065 | ||||||
| chr11:65413133 | T | A | 1 | a0001c0003t0006 | 6 | HG00140.hp1 HG01074.hp1 HG01081.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1773T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 1773 | chr11 | 65413133 | ||||||
| chr11:65413297 | G | A | 1 | a0001c0003t0007 | 4 | HG01069.hp2 HG01071.hp2 NA19009.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1937G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 1937 | chr11 | 65413297 | ||||||
| chr11:65413361 | G | A | 2 | a0001c0007t0013 a0001c0020t0013 |
2 | HG02559.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2001G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 2001 | chr11 | 65413361 | ||||||
| chr11:65413381 | C | T | 1 | a0001c0001t0019 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2021C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 2021 | chr11 | 65413381 | ||||||
| chr11:65413391 | T | G | 1 | a0001c0003t0014 | 2 | HG00323.hp2 HG01255.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2031T>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 2031 | chr11 | 65413391 | ||||||
| chr11:65413412 | A | G | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0016 others(33): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
3_prime_UTR_variant | MODIFIER | c.*2052A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 2052 | chr11 | 65413412 | ||||||
| chr11:65413466 | T | C | 1 | a0001c0002t0011 | 3 | HG03453.hp2 NA18522.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2106T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 2106 | chr11 | 65413466 | ||||||
| chr11:65413471 | T | C | 2 | a0001c0007t0013 a0001c0020t0013 |
2 | HG02559.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2111T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 11/11 | 2111 | chr11 | 65413471 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:65386807 | G | C | 2 | a0001c0002t0001g0016 a0001c0002t0001g0048 |
4 | HG01243.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+46G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 1/10 | chr11 | 65386807 | |||||||
| chr11:65386808 | C | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(211): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.-1+47C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 1/10 | chr11 | 65386808 | |||||||
| chr11:65386846 | CG | C | 11 | a0001c0004t0022g0200 a0001c0007t0003g0015 a0001c0007t0003g0201 others(8): Show |
14 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1+87delG | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 65386846 | ||||||
| chr11:65386955 | C | A | 1 | a0001c0001t0004g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1-82C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 1/10 | chr11 | 65386955 | |||||||
| chr11:65386993 | C | G | 6 | a0001c0005t0002g0004 a0001c0005t0002g0195 a0001c0005t0002g0196 others(3): Show |
13 | HG00735.hp2 HG01070.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1-44C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 1/10 | chr11 | 65386993 | |||||||
| chr11:65387220 | G | C | 1 | a0001c0004t0022g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.85+99G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387220 | |||||||
| chr11:65387232 | A | G | 10 | a0001c0007t0003g0015 a0001c0007t0003g0201 a0001c0007t0003g0202 others(7): Show |
13 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.85+111A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387232 | |||||||
| chr11:65387462 | C | G | 1 | a0001c0004t0022g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.85+341C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387462 | |||||||
| chr11:65387531 | T | C | 1 | a0001c0004t0022g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.85+410T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387531 | |||||||
| chr11:65387624 | C | T | 10 | a0001c0007t0003g0015 a0001c0007t0003g0201 a0001c0007t0003g0202 others(7): Show |
13 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.85+503C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387624 | |||||||
| chr11:65387631 | G | C | 10 | a0001c0007t0003g0015 a0001c0007t0003g0201 a0001c0007t0003g0202 others(7): Show |
13 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.85+510G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387631 | |||||||
| chr11:65387663 | C | G | 1 | a0001c0007t0003g0015 | 4 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+542C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387663 | |||||||
| chr11:65387713 | C | T | 55 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 others(52): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.85+592C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387713 | |||||||
| chr11:65387802 | T | C | 2 | a0001c0001t0001g0026 a0001c0002t0001g0026 |
2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.85+681T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387802 | |||||||
| chr11:65387911 | C | G | 1 | a0001c0004t0022g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.85+790C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387911 | |||||||
| chr11:65387930 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.85+809G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387930 | |||||||
| chr11:65387938 | T | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+817T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387938 | |||||||
| chr11:65387954 | G | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+833G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387954 | |||||||
| chr11:65387957 | A | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+836A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387957 | |||||||
| chr11:65387959 | T | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+838T>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387959 | |||||||
| chr11:65387960 | T | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+839T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387960 | |||||||
| chr11:65387961 | C | T | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+840C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387961 | |||||||
| chr11:65387963 | A | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+842A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387963 | |||||||
| chr11:65387967 | G | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+846G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387967 | |||||||
| chr11:65387970 | G | T | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+849G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387970 | |||||||
| chr11:65387975 | A | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+854A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387975 | |||||||
| chr11:65387977 | C | T | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+856C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387977 | |||||||
| chr11:65387982 | T | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+861T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387982 | |||||||
| chr11:65387985 | A | T | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+864A>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65387985 | |||||||
| chr11:65388010 | G | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+889G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388010 | |||||||
| chr11:65388020 | T | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+899T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388020 | |||||||
| chr11:65388026 | T | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+905T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388026 | |||||||
| chr11:65388026 | T | C | 2 | a0001c0001t0009g0054 a0001c0004t0009g0055 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.85+905T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388026 | |||||||
| chr11:65388033 | A | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+912A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388033 | |||||||
| chr11:65388034 | C | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+913C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388034 | |||||||
| chr11:65388035 | A | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+914A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388035 | |||||||
| chr11:65388036 | T | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+915T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388036 | |||||||
| chr11:65388044 | A | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+923A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388044 | |||||||
| chr11:65388057 | A | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+936A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388057 | |||||||
| chr11:65388079 | A | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+958A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388079 | |||||||
| chr11:65388081 | T | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+960T>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388081 | |||||||
| chr11:65388088 | T | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+967T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388088 | |||||||
| chr11:65388089 | G | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+968G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388089 | |||||||
| chr11:65388092 | A | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+971A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388092 | |||||||
| chr11:65388100 | G | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+979G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388100 | |||||||
| chr11:65388101 | T | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+980T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388101 | |||||||
| chr11:65388105 | G | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+984G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388105 | |||||||
| chr11:65388112 | T | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+991T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388112 | |||||||
| chr11:65388116 | C | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+995C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388116 | |||||||
| chr11:65388118 | C | T | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+997C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388118 | |||||||
| chr11:65388121 | A | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1000A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388121 | |||||||
| chr11:65388125 | T | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1004T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388125 | |||||||
| chr11:65388148 | G | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1027G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388148 | |||||||
| chr11:65388149 | G | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1028G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388149 | |||||||
| chr11:65388151 | T | C | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1030T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388151 | |||||||
| chr11:65388154 | A | G | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1033A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388154 | |||||||
| chr11:65388164 | C | CA | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
8 | HG02280.hp1 HG03831.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.85+1058dupA | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 65388164 | ||||||
| chr11:65388164 | CA | C | 7 | a0001c0001t0001g0159 a0001c0001t0010g0162 a0001c0001t0010g0163 others(4): Show |
7 | HG00544.hp1 HG02622.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+1058delA | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 65388164 | ||||||
| chr11:65388168 | A | G | 3 | a0001c0001t0010g0162 a0001c0001t0010g0163 a0001c0001t0010g0164 |
3 | HG02622.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.85+1047A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388168 | |||||||
| chr11:65388175 | A | C | 10 | a0001c0007t0003g0015 a0001c0007t0003g0201 a0001c0007t0003g0202 others(7): Show |
13 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.85+1054A>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388175 | |||||||
| chr11:65388180 | C | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1059C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388180 | |||||||
| chr11:65388182 | G | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1061G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388182 | |||||||
| chr11:65388183 | G | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1062G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388183 | |||||||
| chr11:65388184 | G | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1063G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388184 | |||||||
| chr11:65388186 | T | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1065T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388186 | |||||||
| chr11:65388187 | C | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1066C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388187 | |||||||
| chr11:65388189 | T | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1068T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388189 | |||||||
| chr11:65388191 | T | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1070T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388191 | |||||||
| chr11:65388192 | C | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1071C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388192 | |||||||
| chr11:65388193 | ATGATCTT others(599): Show |
A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.85+1073_86-562del | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388193 | |||||||
| chr11:65388355 | T | A | 10 | a0001c0007t0003g0015 a0001c0007t0003g0201 a0001c0007t0003g0202 others(7): Show |
13 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.86-1006T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388355 | |||||||
| chr11:65388394 | G | A | 11 | a0001c0004t0022g0200 a0001c0007t0003g0015 a0001c0007t0003g0201 others(8): Show |
14 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.86-967G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388394 | |||||||
| chr11:65388696 | G | C | 1 | a0001c0002t0001g0148 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.86-665G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388696 | |||||||
| chr11:65388718 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0143 |
5 | HG02723.hp2 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-643A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388718 | |||||||
| chr11:65388801 | C | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.86-560C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388801 | |||||||
| chr11:65388802 | C | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.86-559C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388802 | |||||||
| chr11:65388803 | T | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.86-558T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388803 | |||||||
| chr11:65388812 | A | C | 15 | a0001c0001t0010g0162 a0001c0001t0010g0163 a0001c0001t0010g0164 others(12): Show |
18 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.86-549A>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65388812 | |||||||
| chr11:65389003 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0158 |
3 | HG00621.hp1 NA18939.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.86-358A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65389003 | |||||||
| chr11:65389043 | C | T | 1 | a0001c0002t0001g0157 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.86-318C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65389043 | |||||||
| chr11:65389134 | A | G | 15 | a0001c0001t0010g0162 a0001c0001t0010g0163 a0001c0001t0010g0164 others(12): Show |
18 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.86-227A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65389134 | |||||||
| chr11:65389165 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(215): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.86-196T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65389165 | |||||||
| chr11:65389201 | C | G | 1 | a0001c0007t0003g0209 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.86-160C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65389201 | |||||||
| chr11:65389218 | G | A | 3 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 |
3 | HG03453.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.86-143G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 2/10 | chr11 | 65389218 | |||||||
| chr11:65389603 | G | A | 10 | a0001c0007t0003g0015 a0001c0007t0003g0201 a0001c0007t0003g0202 others(7): Show |
13 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.253+75G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65389603 | |||||||
| chr11:65389623 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(78): Show |
145 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.253+95C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65389623 | |||||||
| chr11:65389768 | C | T | 26 | a0001c0001t0002g0103 a0001c0002t0001g0101 a0001c0002t0001g0102 others(23): Show |
40 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.253+240C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65389768 | |||||||
| chr11:65389773 | C | A | 10 | a0001c0007t0003g0015 a0001c0007t0003g0201 a0001c0007t0003g0202 others(7): Show |
13 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.253+245C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65389773 | |||||||
| chr11:65389873 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.253+345G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65389873 | |||||||
| chr11:65390179 | A | G | 11 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0034 others(8): Show |
20 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.253+651A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65390179 | |||||||
| chr11:65390254 | G | T | 1 | a0001c0007t0003g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.253+726G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65390254 | |||||||
| chr11:65390349 | A | G | 59 | a0001c0001t0010g0162 a0001c0001t0010g0163 a0001c0001t0010g0164 others(56): Show |
96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.253+821A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65390349 | |||||||
| chr11:65390414 | G | A | 1 | a0001c0002t0001g0027 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.253+886G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65390414 | |||||||
| chr11:65390476 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.253+948A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65390476 | |||||||
| chr11:65390568 | C | A | 1 | a0001c0007t0003g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.253+1040C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65390568 | |||||||
| chr11:65390772 | G | A | 4 | a0001c0001t0010g0162 a0001c0001t0010g0163 a0001c0001t0010g0164 others(1): Show |
4 | HG02622.hp1 HG06807.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.253+1244G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65390772 | |||||||
| chr11:65390866 | G | A | 2 | a0001c0001t0009g0054 a0001c0004t0009g0055 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.253+1338G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65390866 | |||||||
| chr11:65391180 | C | T | 1 | a0001c0003t0014g0193 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.253+1652C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65391180 | |||||||
| chr11:65391257 | C | G | 1 | a0001c0002t0001g0155 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.253+1729C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65391257 | |||||||
| chr11:65391359 | C | T | 1 | a0001c0004t0002g0105 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.253+1831C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65391359 | |||||||
| chr11:65391360 | C | G | 1 | a0001c0002t0001g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.253+1832C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65391360 | |||||||
| chr11:65391421 | G | A | 1 | a0001c0003t0001g0170 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.253+1893G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65391421 | |||||||
| chr11:65391561 | A | G | 1 | a0005c0013t0001g0080 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.254-2012A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65391561 | |||||||
| chr11:65391678 | T | A | 1 | a0001c0002t0001g0061 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.254-1895T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65391678 | |||||||
| chr11:65391806 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.254-1767C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65391806 | |||||||
| chr11:65391911 | T | C | 52 | a0001c0001t0001g0007 a0001c0001t0001g0107 a0001c0001t0001g0108 others(49): Show |
94 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.254-1662T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65391911 | |||||||
| chr11:65392347 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.254-1226T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65392347 | |||||||
| chr11:65392384 | G | A | 1 | a0001c0003t0001g0044 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.254-1189G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65392384 | |||||||
| chr11:65392394 | T | G | 11 | a0001c0004t0002g0064 a0001c0007t0003g0015 a0001c0007t0003g0201 others(8): Show |
14 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.254-1179T>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65392394 | |||||||
| chr11:65392403 | G | A | 2 | a0001c0007t0003g0202 a0001c0007t0003g0203 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.254-1170G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65392403 | |||||||
| chr11:65392513 | C | G | 1 | a0001c0002t0020g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.254-1060C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65392513 | |||||||
| chr11:65392667 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.254-906C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65392667 | |||||||
| chr11:65392674 | C | T | 46 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 others(43): Show |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.254-899C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65392674 | |||||||
| chr11:65392790 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.254-783T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65392790 | |||||||
| chr11:65393060 | T | G | 1 | a0001c0004t0001g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.254-513T>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65393060 | |||||||
| chr11:65393067 | C | T | 3 | a0001c0001t0010g0162 a0001c0001t0010g0163 a0001c0001t0010g0164 |
3 | HG02622.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.254-506C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65393067 | |||||||
| chr11:65393074 | G | T | 1 | a0001c0001t0002g0103 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.254-499G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65393074 | |||||||
| chr11:65393102 | G | A | 1 | a0001c0010t0001g0028 | 2 | HG02027.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.254-471G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65393102 | |||||||
| chr11:65393271 | A | G | 1 | a0001c0014t0009g0161 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.254-302A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65393271 | |||||||
| chr11:65393535 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.254-38C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65393535 | |||||||
| chr11:65393540 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18951.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.254-33G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 3/10 | chr11 | 65393540 | |||||||
| chr11:65393857 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(159): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.355+183T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 4/10 | chr11 | 65393857 | |||||||
| chr11:65393888 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.356-153G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 4/10 | chr11 | 65393888 | |||||||
| chr11:65393968 | C | A | 1 | a0001c0020t0013g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.356-73C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 4/10 | chr11 | 65393968 | |||||||
| chr11:65393979 | C | T | 2 | a0001c0005t0002g0198 a0001c0005t0002g0199 |
2 | NA18980.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.356-62C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 4/10 | chr11 | 65393979 | |||||||
| chr11:65394160 | C | G | 1 | a0001c0007t0003g0203 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.414+61C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 5/10 | chr11 | 65394160 | |||||||
| chr11:65394893 | T | C | 1 | a0001c0004t0002g0090 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.581+468T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65394893 | |||||||
| chr11:65394909 | G | A | 1 | a0001c0004t0002g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.581+484G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65394909 | |||||||
| chr11:65394937 | C | T | 2 | a0001c0007t0003g0202 a0001c0007t0003g0203 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.581+512C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65394937 | |||||||
| chr11:65394974 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.581+549C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65394974 | |||||||
| chr11:65395017 | C | T | 1 | a0001c0004t0002g0077 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.581+592C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65395017 | |||||||
| chr11:65395026 | C | T | 1 | a0001c0007t0003g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.581+601C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65395026 | |||||||
| chr11:65395246 | T | TA | 8 | a0001c0001t0002g0103 a0001c0001t0010g0162 a0001c0001t0010g0163 others(5): Show |
8 | HG02004.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.581+835dupA | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 65395246 | ||||||
| chr11:65395285 | G | C | 2 | a0001c0001t0009g0054 a0001c0004t0009g0055 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.581+860G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65395285 | |||||||
| chr11:65395309 | G | A | 1 | a0001c0003t0006g0022 | 3 | HG00140.hp1 HG01074.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.581+884G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65395309 | |||||||
| chr11:65395356 | G | A | 1 | a0001c0020t0013g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.581+931G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65395356 | |||||||
| chr11:65395368 | C | T | 2 | a0001c0001t0001g0147 a0001c0002t0001g0148 |
2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.581+943C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65395368 | |||||||
| chr11:65395527 | G | A | 1 | a0001c0020t0013g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.581+1102G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65395527 | |||||||
| chr11:65395821 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0116 |
2 | NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.582-978G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65395821 | |||||||
| chr11:65395968 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.582-831G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65395968 | |||||||
| chr11:65396019 | G | T | 3 | a0001c0002t0001g0021 a0004c0009t0001g0145 a0004c0009t0001g0146 |
5 | HG02630.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.582-780G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396019 | |||||||
| chr11:65396262 | G | T | 1 | a0001c0020t0013g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.582-537G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396262 | |||||||
| chr11:65396296 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.582-503C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396296 | |||||||
| chr11:65396336 | C | T | 1 | a0001c0002t0008g0018 | 3 | HG02572.hp2 HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.582-463C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396336 | |||||||
| chr11:65396354 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.582-445C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396354 | |||||||
| chr11:65396468 | C | T | 1 | a0001c0003t0001g0189 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.582-331C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396468 | |||||||
| chr11:65396494 | G | A | 1 | a0001c0003t0001g0166 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.582-305G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396494 | |||||||
| chr11:65396571 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.582-228C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396571 | |||||||
| chr11:65396614 | G | C | 1 | a0001c0004t0002g0035 | 2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.582-185G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396614 | |||||||
| chr11:65396643 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(96): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.582-156G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396643 | |||||||
| chr11:65396693 | G | T | 1 | a0001c0002t0001g0089 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.582-106G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396693 | |||||||
| chr11:65396734 | C | T | 6 | a0001c0001t0010g0162 a0001c0001t0010g0163 a0001c0001t0010g0164 others(3): Show |
6 | HG02622.hp1 HG03453.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.582-65C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396734 | |||||||
| chr11:65396745 | G | A | 1 | a0001c0002t0001g0135 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.582-54G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 6/10 | chr11 | 65396745 | |||||||
| chr11:65397205 | CAG | C | 9 | a0001c0007t0003g0015 a0001c0007t0003g0201 a0001c0007t0003g0202 others(6): Show |
12 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+186_803+187del others(2): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65397205 | |||||||
| chr11:65397250 | C | T | 2 | a0001c0007t0013g0204 a0001c0020t0013g0078 |
2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.803+230C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65397250 | |||||||
| chr11:65397290 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.803+270C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65397290 | |||||||
| chr11:65397347 | G | A | 3 | a0001c0001t0010g0162 a0001c0001t0010g0163 a0001c0001t0010g0164 |
3 | HG02622.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.803+327G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65397347 | |||||||
| chr11:65397551 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.803+531G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65397551 | |||||||
| chr11:65397628 | G | C | 1 | a0001c0004t0002g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.803+608G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65397628 | |||||||
| chr11:65397634 | A | G | 2 | a0001c0001t0009g0054 a0001c0004t0009g0055 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.803+614A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65397634 | |||||||
| chr11:65397661 | G | A | 1 | a0001c0004t0001g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.803+641G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65397661 | |||||||
| chr11:65397875 | CT | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(138): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.803+873delT | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 65397875 | ||||||
| chr11:65397875 | CTT | C | 8 | a0001c0001t0001g0053 a0001c0001t0001g0107 a0001c0001t0001g0118 others(5): Show |
8 | HG01168.hp1 NA18942.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.803+872_803+873del others(2): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 65397875 | ||||||
| chr11:65397880 | T | C | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0011g0167 others(1): Show |
4 | HG03195.hp2 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+860T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65397880 | |||||||
| chr11:65397974 | C | G | 4 | a0001c0004t0002g0090 a0001c0004t0002g0098 a0001c0004t0002g0099 others(1): Show |
4 | HG00438.hp2 NA18954.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+954C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65397974 | |||||||
| chr11:65398116 | T | C | 1 | a0001c0004t0001g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.803+1096T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65398116 | |||||||
| chr11:65398240 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.803+1220C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65398240 | |||||||
| chr11:65398352 | C | T | 2 | a0001c0001t0001g0039 a0001c0003t0007g0047 |
4 | HG01069.hp2 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+1332C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65398352 | |||||||
| chr11:65398716 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.804-1020C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65398716 | |||||||
| chr11:65398888 | G | A | 1 | a0001c0002t0001g0021 | 3 | HG02630.hp1 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.804-848G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65398888 | |||||||
| chr11:65398925 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.804-811G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65398925 | |||||||
| chr11:65398994 | GT | G | 24 | a0001c0001t0004g0052 a0001c0002t0001g0005 a0001c0002t0001g0011 others(21): Show |
40 | HG00544.hp2 HG00597.hp2 HG02027.hp1 others(37): Show |
intron_variant | MODIFIER | c.804-721delT | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 65398994 | ||||||
| chr11:65398994 | GTT | G | 51 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0002g0103 others(48): Show |
69 | HG00609.hp1 HG00609.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.804-722_804-721del others(2): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 65398994 | ||||||
| chr11:65398994 | GTTT | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(130): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.804-723_804-721del others(3): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 65398994 | ||||||
| chr11:65399289 | G | A | 1 | a0001c0002t0001g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.804-447G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65399289 | |||||||
| chr11:65399378 | C | T | 62 | a0001c0001t0001g0026 a0001c0002t0001g0003 a0001c0002t0001g0005 others(59): Show |
99 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.804-358C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65399378 | |||||||
| chr11:65399541 | G | A | 1 | a0001c0002t0020g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.804-195G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65399541 | |||||||
| chr11:65399546 | C | T | 1 | a0001c0001t0019g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.804-190C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 7/10 | chr11 | 65399546 | |||||||
| chr11:65400069 | G | A | 5 | a0001c0002t0001g0034 a0001c0002t0001g0082 a0001c0002t0001g0085 others(2): Show |
6 | HG00597.hp2 HG02074.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+210G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 8/10 | chr11 | 65400069 | |||||||
| chr11:65400290 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(208): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.927+431A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 8/10 | chr11 | 65400290 | |||||||
| chr11:65400658 | G | C | 1 | a0001c0002t0001g0041 | 2 | HG03834.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.928-66G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 8/10 | chr11 | 65400658 | |||||||
| chr11:65400881 | T | A | 1 | a0001c0003t0001g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1071+14T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65400881 | |||||||
| chr11:65400892 | G | A | 2 | a0001c0001t0009g0054 a0001c0004t0009g0055 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1071+25G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65400892 | |||||||
| chr11:65400979 | G | C | 1 | a0003c0008t0001g0120 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1071+112G>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65400979 | |||||||
| chr11:65401058 | C | A | 1 | a0001c0002t0001g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1071+191C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401058 | |||||||
| chr11:65401068 | A | C | 3 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 |
3 | HG03453.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1071+201A>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401068 | |||||||
| chr11:65401210 | C | T | 1 | a0001c0001t0010g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1071+343C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401210 | |||||||
| chr11:65401235 | C | T | 3 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 |
3 | HG03453.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1071+368C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401235 | |||||||
| chr11:65401298 | TCTACCCC others(6): Show |
T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0007t0013g0204 others(1): Show |
4 | HG02559.hp1 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+433_1071+445d others(15): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 65401298 | ||||||
| chr11:65401300 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(207): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1071+433T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401300 | |||||||
| chr11:65401301 | A | ACCCCAGC others(6): Show |
3 | a0001c0001t0009g0054 a0001c0004t0009g0055 a0001c0014t0009g0161 |
3 | HG01109.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1071+465_1071+477d others(15): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 65401301 | ||||||
| chr11:65401314 | T | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0007t0013g0204 others(1): Show |
4 | HG02559.hp1 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+447T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401314 | |||||||
| chr11:65401322 | C | CTCCCTCC others(19): Show |
2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1071+464_1071+465i others(28): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 65401322 | ||||||
| chr11:65401345 | T | A | 1 | a0001c0014t0009g0161 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1071+478T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401345 | |||||||
| chr11:65401361 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(210): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1071+494C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401361 | |||||||
| chr11:65401374 | T | C | 7 | a0001c0007t0003g0015 a0001c0007t0003g0202 a0001c0007t0003g0203 others(4): Show |
10 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1071+507T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401374 | |||||||
| chr11:65401537 | T | A | 26 | a0001c0001t0002g0103 a0001c0004t0002g0006 a0001c0004t0002g0035 others(23): Show |
40 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1071+670T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401537 | |||||||
| chr11:65401745 | C | G | 4 | a0001c0003t0001g0024 a0001c0003t0001g0104 a0001c0003t0001g0187 others(1): Show |
6 | HG00738.hp1 HG00741.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071+878C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401745 | |||||||
| chr11:65401824 | C | CT | 16 | a0001c0001t0001g0114 a0001c0001t0001g0132 a0001c0001t0001g0158 others(13): Show |
19 | HG00438.hp2 HG01106.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1071+976dupT | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 65401824 | ||||||
| chr11:65401824 | CT | C | 21 | a0001c0001t0001g0037 a0001c0001t0001g0107 a0001c0001t0001g0122 others(18): Show |
21 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1071+976delT | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 65401824 | ||||||
| chr11:65401953 | C | T | 1 | a0001c0004t0002g0095 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1071+1086C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65401953 | |||||||
| chr11:65402037 | C | T | 1 | a0001c0003t0001g0194 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1071+1170C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65402037 | |||||||
| chr11:65402208 | G | A | 1 | a0001c0012t0001g0171 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1071+1341G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65402208 | |||||||
| chr11:65402227 | C | G | 1 | a0001c0004t0002g0077 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1071+1360C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65402227 | |||||||
| chr11:65402279 | G | T | 1 | a0001c0003t0001g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1071+1412G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65402279 | |||||||
| chr11:65402301 | C | T | 1 | a0001c0002t0001g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1071+1434C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65402301 | |||||||
| chr11:65402312 | C | T | 2 | a0001c0007t0013g0204 a0001c0020t0013g0078 |
2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1071+1445C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65402312 | |||||||
| chr11:65402631 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1071+1764C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65402631 | |||||||
| chr11:65402816 | C | CT | 5 | a0001c0002t0001g0016 a0001c0002t0001g0027 a0001c0002t0001g0048 others(2): Show |
8 | HG01243.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1071+1960dupT | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 65402816 | ||||||
| chr11:65402875 | T | C | 1 | a0001c0007t0013g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1072-1989T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65402875 | |||||||
| chr11:65402961 | G | A | 1 | a0001c0007t0013g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1072-1903G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65402961 | |||||||
| chr11:65403129 | T | C | 28 | a0001c0001t0002g0103 a0001c0002t0001g0089 a0001c0004t0002g0006 others(25): Show |
42 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1072-1735T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65403129 | |||||||
| chr11:65403205 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(208): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1072-1659T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65403205 | |||||||
| chr11:65403206 | G | A | 1 | a0001c0007t0003g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1072-1658G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65403206 | |||||||
| chr11:65403276 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1072-1588A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65403276 | |||||||
| chr11:65403340 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(208): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1072-1524A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65403340 | |||||||
| chr11:65403651 | A | C | 1 | a0001c0003t0001g0170 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1072-1213A>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65403651 | |||||||
| chr11:65403652 | G | A | 2 | a0001c0003t0001g0181 a0001c0003t0001g0190 |
2 | NA18959.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1072-1212G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65403652 | |||||||
| chr11:65403684 | T | C | 12 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 others(9): Show |
15 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1072-1180T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65403684 | |||||||
| chr11:65403884 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1072-980T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65403884 | |||||||
| chr11:65403918 | C | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0063 |
3 | NA18968.hp1 NA18998.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1072-946C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65403918 | |||||||
| chr11:65404069 | G | A | 1 | a0001c0001t0001g0042 | 2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1072-795G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65404069 | |||||||
| chr11:65404197 | T | C | 10 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 others(7): Show |
13 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1072-667T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65404197 | |||||||
| chr11:65404435 | C | T | 1 | a0001c0004t0015g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1072-429C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65404435 | |||||||
| chr11:65404532 | C | T | 1 | a0001c0020t0013g0078 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1072-332C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65404532 | |||||||
| chr11:65404556 | C | T | 4 | a0001c0002t0001g0017 a0001c0002t0001g0031 a0001c0002t0001g0056 others(1): Show |
7 | HG02083.hp2 NA18940.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1072-308C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65404556 | |||||||
| chr11:65404668 | C | A | 2 | a0001c0001t0009g0054 a0001c0004t0009g0055 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1072-196C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65404668 | |||||||
| chr11:65404726 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(101): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1072-138C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 9/10 | chr11 | 65404726 | |||||||
| chr11:65405291 | G | T | 1 | a0001c0001t0004g0050 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1276+223G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65405291 | |||||||
| chr11:65405301 | C | T | 1 | a0001c0001t0019g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1276+233C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65405301 | |||||||
| chr11:65405309 | G | A | 1 | a0007c0017t0001g0134 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1276+241G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65405309 | |||||||
| chr11:65405348 | G | A | 10 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 others(7): Show |
13 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276+280G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65405348 | |||||||
| chr11:65405384 | G | A | 2 | a0001c0007t0003g0015 a0001c0011t0003g0205 |
5 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276+316G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65405384 | |||||||
| chr11:65405479 | C | T | 1 | a0001c0004t0022g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1276+411C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65405479 | |||||||
| chr11:65405550 | C | G | 6 | a0001c0002t0001g0017 a0001c0002t0001g0030 a0001c0002t0001g0031 others(3): Show |
10 | HG02083.hp2 NA18940.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.1276+482C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65405550 | |||||||
| chr11:65405596 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0116 |
2 | NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1276+528C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65405596 | |||||||
| chr11:65405650 | G | A | 1 | a0001c0014t0009g0161 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1276+582G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65405650 | |||||||
| chr11:65405691 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1276+623G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65405691 | |||||||
| chr11:65405877 | C | G | 1 | a0001c0014t0009g0161 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1276+809C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65405877 | |||||||
| chr11:65406011 | A | T | 26 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0060 others(23): Show |
37 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1276+943A>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406011 | |||||||
| chr11:65406013 | T | A | 13 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0002g0103 others(10): Show |
17 | HG00408.hp1 HG01106.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1276+945T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406013 | |||||||
| chr11:65406019 | T | A | 1 | a0001c0004t0002g0064 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1276+951T>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406019 | |||||||
| chr11:65406059 | A | G | 1 | a0001c0003t0001g0046 | 2 | HG00140.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1276+991A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406059 | |||||||
| chr11:65406188 | C | T | 1 | a0001c0005t0002g0199 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1276+1120C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406188 | |||||||
| chr11:65406194 | A | AT | 9 | a0001c0001t0001g0060 a0001c0001t0001g0119 a0001c0001t0001g0129 others(6): Show |
9 | HG02135.hp1 HG02602.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.1276+1143dupT | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65406194 | ||||||
| chr11:65406194 | AT | A | 12 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 others(9): Show |
15 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1276+1143delT | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65406194 | ||||||
| chr11:65406283 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(99): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1276+1215C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406283 | |||||||
| chr11:65406415 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0128 others(5): Show |
18 | HG00597.hp1 NA18612.hp1 NA18945.hp2 others(15): Show |
intron_variant | MODIFIER | c.1276+1347C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406415 | |||||||
| chr11:65406501 | T | C | 1 | a0005c0013t0001g0080 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1276+1433T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406501 | |||||||
| chr11:65406529 | C | G | 1 | a0001c0001t0001g0128 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1276+1461C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406529 | |||||||
| chr11:65406556 | C | T | 1 | a0001c0003t0001g0185 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1276+1488C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406556 | |||||||
| chr11:65406608 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1276+1540G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406608 | |||||||
| chr11:65406616 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(208): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1276+1548T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406616 | |||||||
| chr11:65406677 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1276+1609C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406677 | |||||||
| chr11:65406690 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1276+1622A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406690 | |||||||
| chr11:65406738 | G | A | 3 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 |
3 | HG03453.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1276+1670G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406738 | |||||||
| chr11:65406776 | C | T | 2 | a0001c0007t0013g0204 a0001c0020t0013g0078 |
2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1276+1708C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65406776 | |||||||
| chr11:65406940 | C | CAAAT | 3 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 |
3 | HG03453.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1276+1895_1276+189 others(8): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65406940 | ||||||
| chr11:65406940 | CAAAT | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0128 |
5 | HG00597.hp1 NA18945.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276+1895_1276+189 others(8): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65406940 | ||||||
| chr11:65407039 | G | A | 1 | a0001c0003t0001g0182 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1276+1971G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65407039 | |||||||
| chr11:65407228 | CATTT | C | 27 | a0001c0001t0001g0026 a0001c0001t0010g0162 a0001c0002t0001g0003 others(24): Show |
41 | HG00609.hp1 HG00609.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1276+2198_1276+220 others(8): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65407228 | ||||||
| chr11:65407228 | CATTTATT others(1): Show |
C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(166): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1276+2194_1276+220 others(12): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65407228 | ||||||
| chr11:65407228 | CATTTATT others(5): Show |
C | 5 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 others(2): Show |
5 | HG02559.hp1 HG03453.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276+2190_1276+220 others(16): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65407228 | ||||||
| chr11:65407228 | CATTTATT others(9): Show |
C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0014t0009g0161 |
3 | HG06807.hp2 NA18951.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1276+2186_1276+220 others(20): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65407228 | ||||||
| chr11:65407237 | A | G | 1 | a0001c0001t0001g0013 | 4 | HG02723.hp2 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276+2169A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65407237 | |||||||
| chr11:65407240 | T | C | 19 | a0001c0001t0001g0026 a0001c0002t0001g0003 a0001c0002t0001g0021 others(16): Show |
32 | HG00609.hp1 HG00609.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1276+2172T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65407240 | |||||||
| chr11:65407354 | C | A | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1276+2286C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65407354 | |||||||
| chr11:65407385 | GGGATTAC others(6): Show |
G | 1 | a0002c0006t0001g0160 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1276+2319_1276+233 others(17): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65407385 | ||||||
| chr11:65407414 | A | G | 7 | a0001c0007t0003g0015 a0001c0007t0003g0202 a0001c0007t0003g0203 others(4): Show |
10 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1276+2346A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65407414 | |||||||
| chr11:65407618 | T | C | 3 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 |
3 | HG03453.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1276+2550T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65407618 | |||||||
| chr11:65407694 | T | G | 1 | a0001c0004t0002g0064 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1276+2626T>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65407694 | |||||||
| chr11:65407883 | C | CA | 180 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(177): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1276+2831dupA | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65407883 | ||||||
| chr11:65407883 | C | CAA | 13 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0158 others(10): Show |
14 | HG01074.hp2 HG01891.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1276+2830_1276+283 others(6): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65407883 | ||||||
| chr11:65407952 | G | T | 1 | a0001c0004t0002g0096 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1276+2884G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65407952 | |||||||
| chr11:65408059 | T | C | 1 | a0001c0002t0020g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1276+2991T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65408059 | |||||||
| chr11:65408076 | C | CT | 48 | a0001c0001t0001g0026 a0001c0002t0001g0003 a0001c0002t0001g0011 others(45): Show |
72 | HG00609.hp1 HG00609.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1276+3022dupT | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65408076 | ||||||
| chr11:65408076 | C | CTT | 9 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0034 others(6): Show |
18 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.1276+3021_1276+302 others(6): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 65408076 | ||||||
| chr11:65408367 | C | T | 4 | a0001c0002t0001g0061 a0001c0002t0001g0069 a0001c0002t0001g0070 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1277-2875C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65408367 | |||||||
| chr11:65408548 | C | G | 1 | a0001c0004t0002g0067 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1277-2694C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65408548 | |||||||
| chr11:65408575 | A | G | 3 | a0001c0002t0001g0021 a0004c0009t0001g0145 a0004c0009t0001g0146 |
5 | HG02630.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1277-2667A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65408575 | |||||||
| chr11:65408674 | C | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0119 a0001c0001t0001g0158 |
4 | HG00621.hp1 NA18939.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1277-2568C>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65408674 | |||||||
| chr11:65408687 | A | C | 9 | a0001c0007t0003g0015 a0001c0007t0003g0201 a0001c0007t0003g0202 others(6): Show |
12 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1277-2555A>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65408687 | |||||||
| chr11:65408899 | C | T | 28 | a0001c0001t0002g0103 a0001c0004t0001g0065 a0001c0004t0002g0006 others(25): Show |
42 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1277-2343C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65408899 | |||||||
| chr11:65408907 | G | A | 1 | a0001c0002t0008g0018 | 3 | HG02572.hp2 HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1277-2335G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65408907 | |||||||
| chr11:65409049 | G | A | 1 | a0001c0002t0001g0111 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1277-2193G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65409049 | |||||||
| chr11:65409149 | G | T | 2 | a0001c0003t0001g0045 a0001c0003t0001g0180 |
3 | NA18970.hp2 NA18993.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1277-2093G>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65409149 | |||||||
| chr11:65409231 | C | T | 3 | a0001c0002t0011g0167 a0001c0002t0011g0168 a0001c0002t0011g0169 |
3 | HG03453.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1277-2011C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65409231 | |||||||
| chr11:65409248 | G | A | 3 | a0001c0001t0001g0125 a0001c0004t0015g0094 a0001c0004t0015g0097 |
3 | HG02523.hp2 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1277-1994G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65409248 | |||||||
| chr11:65409283 | C | T | 1 | a0001c0014t0009g0161 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1277-1959C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65409283 | |||||||
| chr11:65409701 | G | A | 2 | a0001c0003t0001g0184 a0001c0012t0001g0171 |
2 | HG01361.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1277-1541G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65409701 | |||||||
| chr11:65409799 | C | T | 1 | a0001c0004t0002g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1277-1443C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65409799 | |||||||
| chr11:65409968 | G | A | 50 | a0001c0001t0001g0026 a0001c0002t0001g0003 a0001c0002t0001g0005 others(47): Show |
81 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1277-1274G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65409968 | |||||||
| chr11:65410279 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(211): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1277-963T>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65410279 | |||||||
| chr11:65410405 | G | A | 1 | a0001c0001t0009g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1277-837G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65410405 | |||||||
| chr11:65410667 | G | A | 10 | a0001c0004t0022g0200 a0001c0007t0003g0015 a0001c0007t0003g0201 others(7): Show |
13 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1277-575G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65410667 | |||||||
| chr11:65410683 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(205): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1277-559A>G | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65410683 | |||||||
| chr11:65410726 | CTTGCAGT others(67): Show |
C | 1 | a0001c0002t0001g0048 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1277-515_1277-442d others(76): Show |
FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65410726 | |||||||
| chr11:65410784 | C | T | 1 | a0001c0001t0019g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1277-458C>T | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65410784 | |||||||
| chr11:65410804 | A | C | 1 | a0001c0002t0001g0048 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1277-438A>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65410804 | |||||||
| chr11:65410805 | A | C | 1 | a0001c0002t0001g0048 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1277-437A>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65410805 | |||||||
| chr11:65410806 | A | C | 1 | a0001c0002t0001g0048 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1277-436A>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65410806 | |||||||
| chr11:65410808 | C | A | 1 | a0001c0002t0001g0048 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1277-434C>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65410808 | |||||||
| chr11:65410822 | A | C | 4 | a0001c0001t0001g0042 a0001c0002t0005g0010 a0001c0002t0005g0138 others(1): Show |
9 | HG00735.hp1 HG01069.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1277-420A>C | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65410822 | |||||||
| chr11:65411096 | G | A | 2 | a0001c0007t0013g0204 a0001c0020t0013g0078 |
2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1277-146G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65411096 | |||||||
| chr11:65411149 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(192): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1277-93G>A | FRMD8 | ENSG00000126391.14 | transcript | ENST00000317568.10 | protein_coding | 10/10 | chr11 | 65411149 |